Canonical Allele Identifier: PA658826963
Gene: SLC26A4 HGNC NCBI

Linked Data

ClinVar Variation Id: 550792
ClinVar RCV Id: RCV000665637 RCV002530659
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000432.1:p.Gly497Arg
CA368841280
NM_000441.2:c.1489G>C